I am a Family Physician with > 20 years of clinical research experience, having participated in over 50 clinical trials ranging from phases 1 to 4 in multiple therapeutic areas.After completing my medical residence I had my first contact with clinical research as a sub-investigator. Subsequently, and already within the pharmaceutical industry I covered several positions over the years, beginning with data management of oncology clinical trial data, and then evolving to a monitor profile, project manager of local and multinational clinical studies, and finally clinical research manager.In order to promote clinical research, regulatory compliance, good clinical practices and safeguard the rights and safety of participants I am now dedicated to independent clinical research consulting, providing guidance, training and specialized support both to industry and research centers.I perform project management activities, oversight and monitoring, depending on the clients' needs.Ask me for details to know more about the roles, projects and clients I have worked for as a consultant.Send me an invitation to connect to laura@ardigoconsulting.com or visit my website www.ardigoconsulting.com